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Genetic Elimination of Connective Tissue Growth Factor in the Forebrain Affects Subplate Neurons in the Cortex and Oligodendrocytes in the Underlying White Matter

机译:前脑中结缔组织生长因子的遗传消除影响皮层亚板神经元和基础白质中的少突胶质细胞。

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Connective tissue growth factor (CTGF) is a secreted extracellular matrix-associated protein, which play a role in regulating various cellular functions. Although the expression of CTGF has been reported in the cortical subplate, its function is still not clear. Thus, to explore the significance of CTGF in the brain, we created a forebrain-specific Ctgf knockout (Fb Ctgf KO) mouse model. By crossing Ctgf ~(fl/fl) mice with Emx1-Cre transgenic mice, in which the expression of Cre is prenatally initiated, the full length Ctgf is removed in the forebrain structures. In young adult (2–3 months old) Fb Ctgf KO mice, subplate markers such as Nurr1 and Cplx3 are still expressed in the cortical layer VIb; however, the density of the subplate neurons is increased. Interestingly, in these mutants, we found a reduced structural complexity in the subplate neurons. The distribution patterns of neurons and glial cells, examined by immunohistochemistry, are comparable between genotypes in the somatosensory cortex. However, increased densities of mature oligodendrocytes, but not immature ones, were noticed in the external capsule underneath the cortical layer VIb in young adult Fb Ctgf KO mice. The features of myelinated axons in the external capsule were then examined using electron microscopy. Unexpectedly, the thickness of the myelin sheath was reduced in middle-aged (&12 months old), but not young adult Fb Ctgf KO mice. Our results suggest a secretory function of the subplate neurons, through the release of CTGF, which regulates the density and dendritic branching of subplate neurons as well as the maturation and function of nearby oligodendrocytes in the white matter.
机译:结缔组织生长因子(CTGF)是一种分泌的细胞外基质相关蛋白,在调节各种细胞功能中起作用。尽管已经在皮质亚板中报道了CTGF的表达,但其功能仍不清楚。因此,为了探索CTGF在大脑中的重要性,我们创建了一个前脑特异性Ctgf基因敲除(Fb Ctgf KO)小鼠模型。通过将Ctgf〜(fl / fl)小鼠与Emx1-Cre转基因小鼠杂交,其中Cre的表达是在出生前启动的,全长Ctgf在前脑结构中被去除。在成年(2-3个月大)Fb Ctgf KO小鼠中,皮层VIb中仍表达亚板标记物,例如Nurr1和Cplx3。但是,亚板神经元的密度增加了。有趣的是,在这些突变体中,我们发现亚板神经元的结构复杂性降低了。通过免疫组织化学检查,神经元和神经胶质细胞的分布模式在体感皮层的基因型之间是可比的。但是,在成年的成年Fb Ctgf KO小鼠的皮质层VIb下方的外囊中,发现成熟的少突胶质细胞的密度增加,但未成熟的少突胶质细胞的密度增加。然后使用电子显微镜检查外囊中有髓鞘的轴突的特征。出乎意料的是,在中年(> 12个月大)中,髓鞘的厚度降低了,但是未成年的成年Fb Ctgf KO小鼠中却降低了。我们的研究结果表明,通过释放CTGF,可以调节亚板神经元的分泌功能,从而调节亚板神经元的密度和树突分支以及白质中附近少突胶质细胞的成熟和功能。

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